Self-tuning interfacial architecture for Estradiol detection by surface plasmon resonance biosensor

This study reports the operation principles for reusable SPR biosensors utilizing nanoscale-specific electrostatic levitation phenomena in their sensitive layer design. Functional macromolecular building blocks localized near the "charged" surface by a variety of weak electrostatic interactions create a flexible and structurally variable architecture. A proof-of-concept is demonstrated by an immunospecific detection of 17 beta-Estradiol (E2) following the competitive inhibition format. The sensing interfacial architecture is based on the BSA-E2 conjugate within the BSA matrix immobilized on the "charged" (as a result of guanidine thiocyanate treatment) gold surface at pH 5.0. Kinetic analysis for different E2 concentrations shows that using parameter 13 of the stretched exponential function similar to(1-exp(-(t/tau)(beta)) as an analyte-specific response measure allows one to substantially decrease the low detection limit (down to 10(-3) ng/ml) and increase the dynamic range 10(3) ng/ml) of the SPR biosensor. Finally, it's concluded that the created interfacial architecture is a typical complex system, where SPR response is formed by the stochastic interactions within the whole variety of processes in the system. The E2 addition destroys the uniformity of the reaction space (where an interaction of the antibody (Ab) and the analog of E2 in the self-tuneable matrix takes place) by the redistribution of the immunospecific complexes Ab(E2) (x=0, 1, 2) dependent on E2 concentration. Binding dynamics changes are reflected in the values of beta which summarize in compact form all "hidden" information specific for the evolving distributed interfacial system.